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rs876660812

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660812(G;T)
Make rs876660812(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32341136
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660812
ebirs876660812
HLIrs876660812
Exacrs876660812
Varsomers876660812
Maprs876660812
PheGenIrs876660812
hapmaprs876660812
1000 genomesrs876660812
hgdprs876660812
ensemblrs876660812
gopubmedrs876660812
geneviewrs876660812
scholarrs876660812
googlers876660812
pharmgkbrs876660812
gwascentralrs876660812
openSNPrs876660812
23andMers876660812
23andMe allrs876660812
SNP Nexus

SNPshotrs876660812
SNPdbers876660812
MSV3drs876660812
GWAS Ctlgrs876660812
Max Magnitude0
ClinVar
Risk rs876660812(T;T)
Alt rs876660812(T;T)
Reference rs876660812(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32915273G>T
CLNSRC
CLNACC RCV000216619.1,